Glutamine deprivation induces ferroptosis in pancreatic cancer cells

Ferroptosis is a type of programmed cell death closely related to amino acid metabolism. Pancreatic cancer cells have a strong dependence on glutamine, which serves as a carbon and nitrogen substrate to sustain rapid growth. Glutamine also aids in self-protection mechanisms. However, the effect of glutamine on ferroptosis in pancreatic cancer remains largely unknown. Here, we aim to explore the association between ferroptosis and glutamine deprivation in pancreatic cancer. The growth of pancreatic cancer cells in culture media with or without glutamine is evaluated using Cell Counting Kit-8. Reactive oxygen species (ROS) are measured by 2′,7′-dichlorodihydrofluorescein diacetate staining. Ferroptosis is assessed by BODIPY-C11 dye using confocal microscopy and flow cytometry. Amino acid concentrations are measured using ultrahigh-performance liquid chromatography-tandem mass spectrometry. Isotope-labelled metabolic flux analysis is performed to track the metabolic flow of glutamine. Additionally, RNA sequencing is performed to analyse the genetic alterations. Glutamine deprivation inhibits pancreatic cancer growth and induces ferroptosis both in vitro and in vivo. Additionally, glutamine decreases ROS formation via glutathione production in pancreatic cancer cells. Interestingly, glutamine inhibitors (diazooxonorleucine and azaserine) promotes ROS formation and ferroptosis in pancreatic cancer cells. Furthermore, ferrostatin, a ferroptosis inhibitor, rescues ferroptosis in pancreatic cancer cells. Glutamine deprivation leads to changes in molecular pathways, including cytokine-cytokine receptor interaction pathways ( CCL5, CCR4, LTA, CXCR4, IL-6R, and IL-7R). Thus, exogenous glutamine is required for the detoxification of ROS in pancreatic cancer cells, thereby preventing ferroptosis.


Introduction
Pancreatic ductal adenocarcinoma (PDAC) is one of the most lethal neoplasms, with an average five-year survival rate of less than 10% [1]. Unfortunately, most patients present with unresectable tumors at the time of diagnosis. Only 20% of patients have the opportunity for curative resection [1]. Although surgical interventions have made promising improvements in recent decades, long-term outcomes rely heavily on adjuvant treatments, even in patients with resectable pancreatic cancer [2]. Among the adjuvant treatments, chemotherapy regimens, including FOLFIRINOX and gemcitabine, have shown encouraging results. However, their therapeutic efficacies and side effects remain unsatisfactory [2]. Accurate termination of cancer cells without affecting normal tissues is a difficult goal. Therapies that can selectively target cancer cells are considered promising methods for treating cancers [3]. Since pancreatic cancer cells rely on reprogrammed metabolic pathways to survive and progress, blocking rewired metabolic networks might be an appealing therapeutic approach.
Ferroptosis is a type of regulated cell death dependent on iron. It is genetically and biochemically different from other forms of programmed cell death, such as apoptosis, necroptosis, and autophagy [4]. Ferroptosis is characterized by the accumulation of lipid peroxides. It is initiated by the failure of glutathione-dependent antioxidant defenses, leading to unchecked lipid peroxidation, catastrophic reactive oxygen species (ROS) accumulation, and eventual cell death [5]. Ferroptosis was discovered when a smallmolecule agent, erastin, was identified during screening [6]. Erastin, coined from "Eradicator of RAS-and ST-expressing cells," is selectively detrimental to tumor cells harboring oncogenic RAS mutations [6]. Since KRAS mutations are present in over 90% of pancreatic cancers, they may serve as an ideal model for studying ferroptosis. Moreover, the translational significance is greater considering that KRAS is largely an undruggable target. Interestingly, tumors harboring KRAS mutations have proven to be vulnerable to ferroptosis [7].
Glutamine is the most abundant free amino acid in the human body [8]. Despite being a nonessential amino acid, glutamine, which has been viewed as a nitrogen trap, is an essential source of carbon and nitrogen during the development of cancer [9,10]. Cancer cells consume endogenous and/or exogenous glutamine to support their growth in a context-dependent manner [9]. Compared with other cancer types, pancreatic cancer cells have a stronger dependence on glutamine, as it serves as a source of carbon and nitrogen to fulfil their rapid growth, self-protection mechanisms, invasion, and metastasis [11,12]. For example, glutamine blockade not only suppresses the metabolic programs of pancreatic cancer cells but also enhances their antitumour immune response by modulating CD8 + tumor-infiltrating lymphocytes toward a highly proliferative, activated, and long-lived phenotype [12]. Therefore, the pathways involved in glutamine metabolism could be exploited for therapeutic purposes in pancreatic cancer.
Although glutamate is a proven ferroptosis inhibitor, its effect on ferroptosis in pancreatic cancer has not been extensively studied [4]. In the present, we examined the possible association between ferroptosis and glutamine deprivation. The potential mechanisms involved in ferroptosis induction upon glutamine deprivation were also investigated.

Animal models
Six-week-old female athymic BALB/c nude mice were obtained from the Shanghai Jihui Laboratory Animal Co., Ltd. (Shanghai, China) and maintained in specific pathogen-free facilities according to the approved experimental protocols. The animals were maintained in a temperature-controlled, air-conditioned animal house (20±4°C, 55%±10% humidity). The mice were housed in individual cages in an open-cage system and received food and water ad libitum. The right flanks of the mice were injected subcutaneously with 1×10 6 SW1990 (seven mice in each group) or 1×10 6 BxPC-3 (six mice in each group) pancreatic cancer cells. Mice were randomly assigned to either the diazooxonorleucine (Don) group (750 μg/kg) or the control vehicle group (same volume of saline). The drugs were intraperitoneally administered after inoculation biweekly. The tumor sizes of the xenografts were measured twice a week in length and width using callipers. Tumor volumes were calculated using the following formula: Tumor volume=(long axis) (short axis) 2 π/6. The mice were euthanized using 1% pentobarbital sodium in physiological saline 30 days after tumor inoculation. The tumors were surgically dissected and weighed. The animal study protocol was reviewed and approved by the Ethical Committee of the Fudan University Shanghai Cancer Center (No. FUSCC-IACUC-S20210186).

Cell counting kit-8 (CCK-8) assay
Cell viability was evaluated every 24 h using a Cell Counting Kit-8 (DOJINDO, Kumamoto, Japan) according to the manufacturer's instructions. Briefly, 3000 cells were seeded per well in 96-well plates and cultured for the indicated days. To avoid the influence of the drug on the absorbance, the original medium was removed, and 100 μL of medium containing the CCK-8 reagent was added to the cells and further incubated at 37°C for 2-3 h. Absorbance was measured at 450 nm with a Synergy H4 Hybrid Microplate Reader (BioTek, Winooski, USA). A control was provided for each cell line at the indicated time points.

BODIPY-C11 analysis by confocal microscopy and flow cytometry
For confocal imaging, 10,000 cells were seeded per well in a 24-well plate containing glass slides that were pretreated with polylysine. Cells were treated with glutamine-free medium, medium containing 2 mM glutamine, or medium containing 2 mM glutamine supplemented with 50 μM Don or 10 μM Aza for 72 h. Cells treated with 10 μM RSL3 (Cat. #S8155; Selleck, Housto, USA) or 20 μM erastin (Cat. #HY-15763; MedChemExpress) were used as positive controls. The samples were incubated with 1 μM BODIPY-C11 dye (Cat. #D3861; Thermo Fisher Scientific) for 30 min. After being washed with FBS-free DMEM, the slides were mounted using DAPI Fluoromount-G (Southern Biotech, Birmingham, USA). The cells were imaged at 63× oil magnification using a Leica SP5 II confocal laser scanning microscope (Leica, Wetzlar, Germany). Image analysis was performed using Image-Pro Plus software (Media Cybernetics, Rockville, USA). At least seven randomly selected fields were analyzed per sample. Cells were seeded in 6-well plates for flow cytometry analysis. At the indicated time points, cells were removed along with the medium, washed with prewarmed PBS, and incubated with 5 μM BODIPY-C11 dye diluted in FBS-free DMEM. The cells were washed with DMEM and filtered into single-cell suspensions prior to flow cytometry analysis. Flow cytometry was performed on an FC500 MPL flow cytometer (Beckman Coulter). Oxidized BODIPY-C11 (green emission at 510 nm) was detected. A minimum of 10,000 cells were analyzed for each condition. Data analysis was performed using FlowJo software (version 10.6). The fold increase in BODIPY-C11 + cells was calculated by dividing the percentage of ferroptotic cells in cells cultured in glutamine-free media.

RNA sequencing
RNA sequencing was performed as previously reported with some modifications [14]. Briefly, total RNA was extracted from the cell samples using Trizol reagent (Invitrogen, Carlsbad, USA). Sequencing was conducted on a BGIseq500 platform (BGI-Shenzhen, Shenzhen, China) to obtain single-end 50 base-pair reads. Quality control of the sequencing data was performed using SOAPnuke (v1.5.2). PossionDis with a false discovery rate (FDR)≤0.001 and |Log2Ratio|≥1 were used to assess differential gene expression. Gene set enrichment analysis (GSEA) (http://www.gsea-msigdb. org/) and Kyoto Encyclopedia of Genes and Genomes (KEGG) (https://www.kegg.jp/) enrichment analysis of the differentially expressed genes were performed.

Isotope labelled metabolic flux analysis
SU.8686 cells were cultured for 12 or 24 h in media containing Lglutamine-15 N 2 (Cat. #490032; Sigma-Aldrich) or L-Glutamine-13 C 5 (Cat. #605166; Sigma-Aldrich). Cells cultured in unlabelled glutamine were used as controls. A total of 1×10 7 cells were collected for analysis. For sample preparation, 1000 μL of extraction solution (acetonitrile:methanol:water=2:2:1) containing an isotopically labelled internal standard mixture was added to the sample. LC-MS/MS analyses were performed using a UHPLC System (1290; Agilent Technologies) with a UPLC HSS T3 column (2.1 mm× 100 mm, 1.8 μm) coupled to a Q Exactive mass spectrometer (Thermo Fisher Scientific). The raw data were converted to the mzXML format using ProteoWizard and processed with an in-house program that was developed using R and based on XCMS for peak detection, extraction, alignment, and integration [16]. M+ (M0, M1 to Mn) represents the number of C or N atoms in the metabolites labelled by the isotopes. The fractional abundances of the mass isotopomers defined by M0, M1, and Mn were calculated.

Statistical analysis
Data are expressed as the mean±SEM unless otherwise indicated. Statistical analyses were conducted using SPSS software (version 19.0; IBM Corp., Armonk, USA) and Prism statistical software (version 8; GraphPad Software, Inc., La Jolla, USA). Unpaired twotailed Student's t test was used to compare the data between the two groups. For multiple comparisons, ANOVA combined with the Bonferroni correction was used. Significance was defined as a P value <0.05, unless otherwise stated.

Glutamine deprivation inhibits pancreatic cancer growth
The avidity of glutamine for cancer cells has been well recognized because glutamine is a common component of cell culture media. To examine the effect of glutamine on pancreatic cancer growth, the proliferation of pancreatic cancer cells (SW1990 and SU.8686) at

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Glutamine deprivation induces pancreatic cancer ferroptosis different time points was determined by CCK-8. Glutamine enhanced the proliferation of pancreatic cancer cells, which was inhibited by Don ( Figure 1A,B). In addition, glutamine blockade using Don inhibited tumor volume and weight in SW1990 and BxPC-3 mouse xenograft models ( Figure 1C-I). Therefore, glutamine is an essential nutrient for the progression of pancreatic cancer.

Glutamine starvation induces ferroptosis in pancreatic cancer cells
BODIPY-C11 is a lipid peroxidation sensor used to detect ROS in cells and membranes, with good spectral separation of the nonoxidized (590 nm) and oxidized (510 nm) forms [17]. To investigate the effect of glutamine starvation on ferroptosis in pancreatic cancer cells, BODIPY-C11+ cells were assessed by immunofluorescence assay and flow cytometry. Ferroptosis-inducing agents (RSL3 and erastin) were used as positive controls. The levels of ferroptosis in SW1990 and SU.8686 cells deprived of glutamine were higher than those in cells supplemented with 2 mM glutamine as revealed by confocal laser scanning microscopy ( Figure 2A,B). Additionally, glutamine inhibitors (Don and Aza) induced ferroptosis in pancreatic cancer cells (Figure 2A,B). The same trend of glutamine-induced ferroptosis in pancreatic cancer cells was confirmed by flow cytometry (Figure 2C-F). A major proportion of ferroptotic cells were lost during the washing process of the immunofluorescence assay, and ferroptosis was more evident in the erastin group. This led to an inconsistency between the Erastin and RSL3 controls that underwent immunofluorescence and flow cytometry assays. The inhibitors of apoptosis (Z-VAD-FMK) and necroptosis (necrostatin-1) failed to block glutamine starvationinduced lipid oxidation in SW1990 ( Figure 3A,C,D) and SU.8686 cells ( Figure 3B,E,F). In contrast, the ferroptosis inhibitor ferrostatin-1 efficiently blocked cell lipid oxidation in response to glutamine starvation ( Figure 3C-F). The ferroptosis inhibitor NAC efficiently blocked lipid oxidation in SU.8686 cells, but not in SW1990 cells, in response to glutamine starvation. Therefore, glutamine deprivation induces ferroptosis in pancreatic cancer cells in vitro.

Deprivation of glutamine induces ferroptosis in pancreatic cancer in vivo
Lipid droplet accumulation is a feature of ferroptosis in cancer cells and can be directly observed by histopathological examination. The accumulation of lipid droplets is related to the induction of ferroptosis [18,19]. In clear cell renal cell carcinoma, acyl-CoA synthetase 3 (ACSL3) could regulate ferroptosis susceptibility in a manner dependent on lipid droplet accumulation by metabolizing exogenously derived lipids [19]. Inhibition of ACSL3 reduces the sensitivity of cancer cells to ferroptotic cell death. To examine glutamine inhibition-induced ferroptosis in vivo, xenograft mouse models, developed by injecting pancreatic cancer cells, were treated with saline or Don. Athymic BALB/c nude mice were subcutaneously inoculated with SW1990 or BxPC-3 cells. Hematoxylin and eosin (H&E) staining revealed increased lipid peroxide droplet accumulation in the Don group compared to the control group (Figure 4), indicating that deprivation of glutamine induces ferroptosis in pancreatic cancer cells in vivo.

Glutamine decreases ROS production in pancreatic cancer cells
Previous studies have indicated that glutamine deficiency increases ROS levels in cancer cells [18]. DCFH-DA is one of the most commonly used probes for quantifying cellular H 2 O 2 and ROS [19].
To evaluate the effect of glutamine deficiency on ROS production during pancreatic cancer, SW1990, BxPC-3, and SU.8686 cells were cultured in media with varying concentrations of glutamine (0, 1, 2, 4, and 10 mM) and examined by DCFH-DA assay using flow cytometry. Since commercially available media usually contain 2 mM glutamine, cells were cultured for different durations (24,48, and 72 h) in media containing 2 mM glutamine. Glutamine inhibited ROS formation in pancreatic cancer cells in a concentration-dependent manner ( Figure 5A-C). The decrease in ROS was more evident when the cells were cultured for 48 or 72 h ( Figure  5D-F). BxPC-3 cells were more dependent on glutamine than SW1990 and SU.8686 cells. Thus, glutamine decreases ROS production in pancreatic cancer cells.

Glutamine decreases ROS formation via reduced glutathione (GSH) production in pancreatic cancer cells
Glutathione (GSH) aids in the neutralization of free radicals and is important for protecting cells against oxidative stress and toxic xenobiotics. The effect of glutamine on ROS production may be associated with GSH and oxidized glutathione (GSSG) production.
To test this hypothesis, fractional isotopomer labelling of GSH and GSSG with [U-13 C]-L-glutamine or [U-15 N]-L-glutamine was examined by UHPLC in SU.8686 cells cultured for 12 and 24 h. Next, isotope-labelled glutamine was traced in the GSH and GSSG produced ( Figure 6A-D). The concentration of GSH, measured by UHPLC-MS/MS, was higher in SW1990 and BxPC-3 cells treated with medium containing 2 mM glutamine than in cells cultured in glutamine-free media for 24 h but not for 48 h ( Figure 6E,F). Glutamine supplementation was not associated with GSSG production in cells cultured for 24 h or 48 h (data not shown). The deprivation of glutamine led to a decrease in intracellular GSH at 24 h and an increase in intracellular ROS at 48 h. This could be explained by the production of GSH being decreased at first and the ROS levels subsequently increased [20]. Thus, glutamine blockade promotes ROS formation by reducing GSH but not GSSG in pancreatic cancer cells.

Glutamine blockade promotes ROS formation in pancreatic cancer cells
Our results have shown that glutamine decreases ferroptosis in pancreatic cancer, which can be reversed by glutamine inhibitors such as Don and Aza. To confirm that these inhibitors induce ferroptosis by promoting ROS levels, the proportion of DCFH-DA was evaluated in SW1990, BxPC-3, and SU.8686 cells cultured in media containing 2 mM glutamine and treated with Don or Aza for 72 h. Glutamine blockade promoted ROS formation in pancreatic cancer cells (SW1990 and SU.8686), as measured by flow cytometry (Figure 7).

Potential molecular pathways involved in glutamine deprivation-induced ferroptosis
To

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Glutamine deprivation induces pancreatic cancer ferroptosis  pathway (PPP), a metabolic pathway parallel to glycolysis that produces precursors for nucleotide synthesis, was enriched by GSEA, suggesting that glutamine supplies substrates for pancreatic cancer growth ( Figure 8A). Peroxisome proliferator-activated receptors (PPARs), which play essential roles in the regulation of cellular differentiation, development, metabolism (carbohydrates, lipids, and proteins), and tumorigenesis, were also enriched ( Figure 8B). Tumor cells can reprogram their metabolism under nutrientdeprived conditions. In this study, the cytokine-cytokine receptor interaction pathway was the most enriched pathway between pancreatic cancer cells treated with and without glutamine, including CCL5, CCR4, LTA, CXCR4, IL-6R, and IL-7R ( Figure  8C). The differential expression of IL6R and CXCR4 was confirmed by qRT-PCR ( Figure 8D,E). Therefore, pancreatic cancer cells may secrete cytokines under glutamine deprivation conditions to recruit stromal or immune cells to cope with nutrient crises.

Discussion
Glutamine is a super nutrient for pancreatic cancer growth and progression [10,12]. In this study, we demonstrated that glutamine deprivation inhibits pancreatic cancer growth by inducing ferroptosis, which may be associated with ROS production. Glutamine inhibitors increase ferroptosis in pancreatic cancer cells. Induction of ferroptosis upon glutamine deprivation can be rescued by a ferroptosis inhibitor (ferrostatin-1) but not by apoptosis inhibitor (Z-VAD-FMK) or necroptosis inhibitor (necrostatin-1). Signaling pathways, including PPP, PPARs, and cytokine-cytokine receptor interactions, were enriched in glutamine-starved cells. Therefore, pancreatic cancer cells require exogenous glutamine to prevent ferroptosis. Glutamine deprivation reduces GSH production and promotes ROS production, which may induce ferroptosis in pancreatic cancer cells (Figure 9). However, further studies are needed to explore the association between glutamine deprivation and ferroptosis in pancreatic cancer cells.
Ferroptosis has been demonstrated to be associated with metabolism, redox biology, and cancer [4,5]. Triggering ferroptosis is a potential strategy for cancer treatment [4,21]. Previous reports have suggested a potential connection between glutamine and ferroptosis [18]. Glutamine-fueled intracellular metabolic pathways play an essential role in ferroptosis through the product of glutaminolysis, α-ketoglutarate (α-KG) [18]. Accumulation of

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Glutamine deprivation induces pancreatic cancer ferroptosis extracellular glutamate, an interacting form of glutamine, can stimulate ferroptosis in physiological contexts [22]. Our study confirms that glutamine deprivation activates ferroptosis in pancreatic cancer cells. Glutamine deprivation is closely related to ROS production, which induces ferroptosis in tumors [11,22,23]. ROS levels are dynamically modulated throughout pancreatic cancer progression, with lower levels of ROS accelerating tumor initiation in premalignant conditions and higher levels promoting metastatic progression [24]. Although ROS is pro-tumorigenic, high ROS levels are cytotoxic to cancer cells [22]. Tumor cells express increased levels of antioxidant proteins to detoxify ROS, suggesting that a delicate balance in intracellular ROS levels is required for optimal cancer cell function. Upon the modulation of oncogenic KRAS, glutamine is converted into oxaloacetate by aspartate transaminase and further into pyruvate, which increases the NADPH/NADP + ratio to preserve cellular redox balance [11]. Our study confirmed a previous report showing that glutamine deprivation results in an increase in ROS and a decrease in GSH levels [11]. Meanwhile, the percentage of DCFH-DA + cells shows a decreasing trend over time in pancreatic cancer cells cultured in glutamine-free media, which may be caused by the adaptation of cells to glutamine deprivation through glutamine anaplerotic reactions [8].
Thus, the association between glutamine deprivation and ROS production may be related to cysteine production. Cysteine is a source of glutathione synthesis that participates in counteracting ROS production through oncogenic signaling. Cyst(e)ine supplementation promotes colon cancer growth and chemoresistance by activating mTORC1 via GCN2-ATF4. This quenches chemotherapy-induced ROS via the synthesis of glutathione [25]. Glutamate, cysteine, and glycine are precursor amino acids involved in GSH synthesis. Inhibition of cytosolic aspartate aminotransaminase

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Glutamine deprivation induces pancreatic cancer ferroptosis (GOT1) enhances pancreatic cancer cell death via ferroptosis. Furthermore, cysteine, glutathione, and lipid antioxidants function as metabolic vulnerabilities following GOT1 blockade [26]. Glutamate is exchanged for cystine in a 1:1 ratio by system Xc _ , a plasma membrane transporter. Thus, glutamate or glutamine level may impact ferroptosis through cysteine transport [4]. A previous study showed that cysteine depletion could induce pancreatic cancer ferroptosis in genetically engineered mice and inhibit pancreatic cancer growth by mediating the synthesis of GSH and coenzyme A [21]. The deletion of a system Xc _ subunit, SLC7A11, or a combination of GSH and coenzyme A blockade, or the administration of cyst(e)inases, could induce tumor-selective ferroptosis [21]. Therefore, we suggest that glutamine is an essential nutritional source that not only supports pancreatic cancer growth but also prevents the induction of ferroptosis. However, further studies are needed to elucidate the mechanism of glutamine deprivationinduced cell death. This study indicates a potential connection between glutamine, cysteine, GSH, ROS, and ferroptosis in pancreatic cancer. However, the potential molecules regulating this metabolic pathway need to be further identified. Nuclear factor erythroid 2-related factor 2 (NRF2) is a basic leucine zipper protein and master regulator of the cellular antioxidant response [27]. It is a transcription factor that regulates the expressions of antioxidant proteins that protect cells against ROS damage triggered by injury and inflammation [27]. ROS levels are tightly regulated by the NRF2/Kelch-like ECH-associated protein 1 (KEAP1) interaction under normal physiological conditions. In pancreatic cancer, mutations in the KRAS proto-oncogene are present in over 90% of cases and are associated with tumor proliferation and cellular metabolism. A byproduct of KRAS oncogenic activation is the increased production of ROS, which is harmful to cellular components. To compensate for this, the KRAS G12D mutation increases the constitutive transcription of NRF2 to disrupt the NRF2-KEAP1 interaction, thereby actively suppressing intracellular ROS via the Raf-MEK-ERK-Jun pathway [28]. Thus, enhanced ROS detoxification and the antioxidant function of NRF2 may play an unappreciated role in tumorigenesis. KRAS/NRF2and KRAS/KEAP1-mutant lung cancers are sensitive to reduced glutamine levels [7]. Moreover, nutrient deprivation is sufficient to enhance the biosynthesis and/or secretion of specific proinflammatory cytokines to trigger adaptive responses [29]. A previous study showed that glutamine restriction stimulates the release of IL-6 and IL-8, which further recruits B cells, macrophages, and neutrophils. Our study shows that the cytokine-cytokine receptor interaction pathway is enriched under glutamine deprivation, indicating that pancreatic cancer cells may secrete cytokines to recruit stromal cells to cope with glutamine deprivation. The association between glutamine deprivation, NRF2/KEAP1, and cytokine secretion in KRAS-mutant pancreatic cancer warrants further investigation. The distinctive effects of NAC on ferroptosis may be explained by the differential expression of KRAS (SW1990, KRAS low; SU.8686 KRAS high), which plays a key role in Figure 9. Schematic illustration of how glutamine promotes pancreatic cancer progression by inhibiting reactive oxygen species (ROS)-related ferroptosis Glutamine deprivation reduces GSH production and promotes ROS production, which may trigger ferroptosis in pancreatic cancer cells.
In summary, glutamine has been confirmed to be a critical nutrient for the oncogenesis and progression of pancreatic cancer. Our study further demonstrates that glutamine deprivation can induce pancreatic cancer ferroptosis. This provides necessary evidence to explore the efficacy of glutamine blockade in pancreatic cancer. However, since glutamine is an important nutrient for the human body, the delicate balance between its antitumour effect and potential toxicity remains to be explored. Further studies are required to elucidate the mechanism by which necrostatin-1 induces ferroptosis in pancreatic cancer cells.